rs45476696
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs45476696(A;A) |
Make rs45476696(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 21970902 |
Gene | CDKN2A |
is a | snp |
is | mentioned by |
dbSNP | rs45476696 |
dbSNP (classic) | rs45476696 |
ClinGen | rs45476696 |
ebi | rs45476696 |
HLI | rs45476696 |
Exac | rs45476696 |
Gnomad | rs45476696 |
Varsome | rs45476696 |
LitVar | rs45476696 |
Map | rs45476696 |
PheGenI | rs45476696 |
Biobank | rs45476696 |
1000 genomes | rs45476696 |
hgdp | rs45476696 |
ensembl | rs45476696 |
geneview | rs45476696 |
scholar | rs45476696 |
rs45476696 | |
pharmgkb | rs45476696 |
gwascentral | rs45476696 |
openSNP | rs45476696 |
23andMe | rs45476696 |
SNPshot | rs45476696 |
SNPdbe | rs45476696 |
MSV3d | rs45476696 |
GWAS Ctlg | rs45476696 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs45476696(A;A) rs45476696(T;T) |
Alt | rs45476696(A;A) rs45476696(T;T) |
Reference | Rs45476696(G;G) |
Significance | Pathogenic |
Disease | Hereditary cutaneous melanoma Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | CDKN2A |
CLNDBN | Hereditary cutaneous melanoma Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000009.11:g.21970901C>A |
CLNSRC | |
CLNACC | RCV000198192.3, RCV000223581.2, |